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{{Infobox_gene}}
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'''Filamin B, beta''' (FLNB), also known as '''Filamin B, beta (actin binding protein 278)''', is a [[cytoplasm]]ic [[protein]] which in humans is encoded by the ''FLNB'' [[gene]].
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FLNB regulates intracellular communication and signalling by cross-linking the protein [[actin]] to allow direct communication between the [[cell membrane]] and [[cytoskeleton|cytoskeletal network]], to control and guide proper skeletal development.<ref name=filb>{{cite journal |vauthors=Lu J, Lian G, Lenkinski R, De Grand A, Vaid RR, Bryce T, Stasenko M, Boskey A, Walsh C, Sheen V |title=Filamin B mutations cause chondrocyte defects in skeletal development |journal=Hum Mol Genet |volume=16 |issue=14 |pages=1661–1675 |year=2007 |pmid=17510210 |doi=10.1093/hmg/ddm114 }}</ref>
{{GNF_Protein_box
| image = PBB_Protein_FLNB_image.jpg
| image_source = [[Protein_Data_Bank|PDB]] rendering based on 2di8.
| PDB = {{PDB2|2di8}}, {{PDB2|2di9}}, {{PDB2|2dia}}, {{PDB2|2dib}}, {{PDB2|2dic}}, {{PDB2|2dj4}}, {{PDB2|2dlg}}, {{PDB2|2dmb}}, {{PDB2|2dmc}}
| Name = Filamin B, beta (actin binding protein 278)
| HGNCid = 3755
| Symbol = FLNB
| AltSymbols =; ABP-278; AOI; DKFZp686A1668; DKFZp686O033; FH1; FLN1L; LRS1; SCT; TABP; TAP; filamin B
| OMIM = 603381
| ECnumber = 
| Homologene = 37480
| MGIid = 2446089
| GeneAtlas_image1 = PBB_GE_FLNB_208614_s_at_tn.png
| GeneAtlas_image2 = PBB_GE_FLNB_208613_s_at_tn.png
| Function = {{GNF_GO|id=GO:0003779 |text = actin binding}} {{GNF_GO|id=GO:0005515 |text = protein binding}}
| Component = {{GNF_GO|id=GO:0015629 |text = actin cytoskeleton}} {{GNF_GO|id=GO:0016021 |text = integral to membrane}}
| Process = {{GNF_GO|id=GO:0007016 |text = cytoskeletal anchoring}} {{GNF_GO|id=GO:0007165 |text = signal transduction}} {{GNF_GO|id=GO:0007275 |text = multicellular organismal development}} {{GNF_GO|id=GO:0007519 |text = striated muscle development}} {{GNF_GO|id=GO:0030036 |text = actin cytoskeleton organization and biogenesis}} {{GNF_GO|id=GO:0030154 |text = cell differentiation}}
| Orthologs = {{GNF_Ortholog_box
    | Hs_EntrezGene = 2317
    | Hs_Ensembl = ENSG00000136068
    | Hs_RefseqProtein = NP_001448
    | Hs_RefseqmRNA = NM_001457
    | Hs_GenLoc_db = 
    | Hs_GenLoc_chr = 3
    | Hs_GenLoc_start = 57969167
    | Hs_GenLoc_end = 58133015
    | Hs_Uniprot = O75369
    | Mm_EntrezGene = 286940
    | Mm_Ensembl = ENSMUSG00000025278
    | Mm_RefseqmRNA = XM_487363
    | Mm_RefseqProtein = XP_487363
    | Mm_GenLoc_db = 
    | Mm_GenLoc_chr = 14
    | Mm_GenLoc_start = 6608561
    | Mm_GenLoc_end = 6743464
    | Mm_Uniprot = Q3T9V9
  }}
}}
'''Filamin B, beta (actin binding protein 278)''', also known as '''FLNB''', is a human [[cytoplasm]]ic [[protein]].<ref name="entrez">{{cite web | title = Entrez Gene: FLNB filamin B, beta (actin binding protein 278)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2317| accessdate = }}</ref> It regulates intracellular communication and signalling by cross-linking the protein [[actin]] to allow direct communication between the [[cell membrane]] and [[cytoskeleton|cytoskeletal network]], to control and guide proper skeletal development.<ref name=filb>{{cite journal |author=Lu J, Lian G, Lenkinski R, De Grand A, Vaid RR, Bryce T, Stasenko M, Boskey A, Walsh C, Sheen V |title=Filamin B mutations cause chondrocyte defects in skeletal development |journal=Hum Mol Genet. |volume=16 |issue=14 |pages=1661-1675 |year=2007 |pmid=17510210 }}</ref>


Mutations in the FLNB gene are involved in several [[osteochondrodysplasia|lethal bone dysplasias]], including [[boomerang dysplasia]] and [[atelosteogenesis type I]].<ref name=mutbd>{{cite journal |author=Bicknell LS, Morgan T, Bonife L, Wessels MW, Bialer MG, Willems PJ, Cohen DH, Krakow D, Robertson SP |title=Mutations in FLNB cause boomerang dysplasia |journal=Am J Med Genet. |volume=42 |issue=7 |pages=e43 |year=2005 |pmid=15994868}}</ref><ref name=lbdys>{{cite journal |author=Greally MT, Jewett T, Smith WL Jr., Penick GD, Williamson RA |title=Lethal bone dysplasia in a fetus with manifestations of Atelosteogenesis type I and Boomerang dysplasia |journal=Am J Med Genet. |volume=47 |issue=4 |pages=1086-1091 |year=1993 |pmid=8291529 }}</ref><ref name=bddom>{{cite journal |author=Nishimura G, Horiuchi T, Kim OH, Sasamoto Y |title=Atypical skeletal changes in otopalatodigital syndrome type II: phenotypic overlap among otopalatodigital syndrome type II, boomerang dysplasia, atelosteogenesis type I and type III, and lethal male phenotype of of Melnick-Needles syndrome |journal=Am J Med Genet. |volume=73 |issue=2 |pages=132-138 |year=1997 |pmid=9409862 }}</ref>
Mutations in the FLNB gene are involved in several [[osteochondrodysplasia|lethal bone dysplasias]], including [[boomerang dysplasia]] and [[atelosteogenesis type I]].<ref name=mutbd>{{cite journal |vauthors=Bicknell LS, Morgan T, Bonife L, Wessels MW, Bialer MG, Willems PJ, Cohen DH, Krakow D, Robertson SP |title=Mutations in FLNB cause boomerang dysplasia |journal=Am J Med Genet |volume=42 |issue=7 |pages=e43 |year=2005 |pmid=15994868 |doi=10.1136/jmg.2004.029967 |pmc=1736093}}</ref><ref name=lbdys>{{cite journal |author1=Greally MT |author2=Jewett T |author3=Smith WL Jr. |author4=Penick GD |author5=Williamson RA |title=Lethal bone dysplasia in a fetus with manifestations of Atelosteogenesis type I and Boomerang dysplasia |journal=Am J Med Genet |volume=47 |issue=4 |pages=1086–1091 |year=1993 |pmid=8291529 |doi=10.1002/ajmg.1320470731 }}</ref><ref name=bddom>{{cite journal |vauthors=Nishimura G, Horiuchi T, Kim OH, Sasamoto Y |title=Atypical skeletal changes in otopalatodigital syndrome type II: phenotypic overlap among otopalatodigital syndrome type II, boomerang dysplasia, atelosteogenesis type I and type III, and lethal male phenotype of Melnick-Needles syndrome |journal=Am J Med Genet |volume=73 |issue=2 |pages=132–138 |year=1997 |pmid=9409862 |doi=10.1002/(SICI)1096-8628(19971212)73:2<132::AID-AJMG6>3.0.CO;2-W }}</ref>
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{{PBB_Summary
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==Interactions==
FLNB has been shown to [[Protein-protein interaction|interact]] with [[GP1BA]],<ref name=pmid9651345>{{cite journal |last=Takafuta |first=T |authorlink= |author2=Wu G |author3=Murphy G F |author4=Shapiro S S  |date=Jul 1998 |title=Human beta-filamin is a new protein that interacts with the cytoplasmic tail of glycoprotein Ibalpha |journal=J. Biol. Chem. |volume=273 |issue=28 |pages=17531–8 |publisher= |location = UNITED STATES| issn = 0021-9258| pmid = 9651345 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = |doi=10.1074/jbc.273.28.17531 }}</ref> [[Filamin]],<ref name=pmid12393796>{{cite journal |last=Sheen |first=Volney L |authorlink= |author2=Feng Yuanyi |author3=Graham Donna |author4=Takafuta Toshiro |author5=Shapiro Sandor S |author6=Walsh Christopher A  |date=Nov 2002 |title=Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interact |journal=Hum. Mol. Genet. |volume=11 |issue=23 |pages=2845–54 |publisher= |location = England| issn = 0964-6906| pmid = 12393796 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = |doi=10.1093/hmg/11.23.2845 }}</ref> [[FBLIM1]],<ref name=pmid12496242>{{cite journal |last=Takafuta |first=Toshiro |authorlink= |author2=Saeki Mari |author3=Fujimoto Tetsuro-Takahiro |author4=Fujimura Kingo |author5=Shapiro Sandor S  |date=Apr 2003 |title=A new member of the LIM protein family binds to filamin B and localizes at stress fibers |journal=J. Biol. Chem. |volume=278 |issue=14 |pages=12175–81 |publisher= |location = United States| issn = 0021-9258| pmid = 12496242 |doi = 10.1074/jbc.M209339200 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = }}</ref> [[PSEN1]],<ref name=pmid9437013>{{cite journal |last=Zhang |first=W |authorlink= |author2=Han S W |author3=McKeel D W |author4=Goate A |author5=Wu J Y  |date=Feb 1998 |title=Interaction of presenilins with the filamin family of actin-binding proteins |journal=J. Neurosci. |volume=18 |issue=3 |pages=914–22 |publisher= |location = UNITED STATES| issn = 0270-6474| pmid = 9437013 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = |pmc=2042137 }}</ref> [[CD29]]<ref name=pmid11807098>{{cite journal |last=van der Flier |first=Arjan |authorlink= |author2=Kuikman Ingrid |author3=Kramer Duco |author4=Geerts Dirk |author5=Kreft Maaike |author6=Takafuta Toshiro |author7=Shapiro Sandor S |author8=Sonnenberg Arnoud  |date=Jan 2002 |title=Different splice variants of filamin-B affect myogenesis, subcellular distribution, and determine binding to integrin [beta] subunits |journal=J. Cell Biol. |volume=156 |issue=2 |pages=361–76 |publisher= |location = United States| issn = 0021-9525| pmid = 11807098 |doi = 10.1083/jcb.200103037 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = |pmc=2199218 }}</ref> and [[PSEN2]].<ref name=pmid9437013/>
==See also==
* [[Larsen syndrome]]
==References==
==References==
{{reflist|2}}
{{reflist}}
 
==External links==
*[https://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=flnb-dis  GeneReview/NIH/UW entry on FLNB-Related Disorders]


==Further reading==
==Further reading==
{{refbegin | 2}}
{{refbegin | 2}}
{{PBB_Further_reading  
{{PBB_Further_reading
| citations =  
| citations =
*{{cite journal  | author=Stossel TP, Condeelis J, Cooley L, ''et al.'' |title=Filamins as integrators of cell mechanics and signalling. |journal=Nat. Rev. Mol. Cell Biol. |volume=2 |issue= 2 |pages= 138-45 |year= 2001 |pmid= 11252955 |doi= 10.1038/35052082 }}
*{{cite journal  |vauthors=Stossel TP, Condeelis J, Cooley L |title=Filamins as integrators of cell mechanics and signalling. |journal=Nat. Rev. Mol. Cell Biol. |volume=2 |issue= 2 |pages= 138–45 |year= 2001 |pmid= 11252955 |doi= 10.1038/35052082 |display-authors=etal}}
*{{cite journal  | author=van der Flier A, Sonnenberg A |title=Structural and functional aspects of filamins. |journal=Biochim. Biophys. Acta |volume=1538 |issue= 2-3 |pages= 99-117 |year= 2001 |pmid= 11336782 |doi=  }}
*{{cite journal  |vauthors=van der Flier A, Sonnenberg A |title=Structural and functional aspects of filamins. |journal=Biochim. Biophys. Acta |volume=1538 |issue= 2–3 |pages= 99–117 |year= 2001 |pmid= 11336782 |doi=10.1016/S0167-4889(01)00072-6 }}
*{{cite journal  | author=Vujic M, Hallstensson K, Wahlström J, ''et al.'' |title=Localization of a gene for autosomal dominant Larsen syndrome to chromosome region 3p21.1-14.1 in the proximity of, but distinct from, the COL7A1 locus. |journal=Am. J. Hum. Genet. |volume=57 |issue= 5 |pages= 1104-13 |year= 1995 |pmid= 7485161 |doi=  }}
*{{cite journal  |vauthors=Vujic M, Hallstensson K, Wahlström J |title=Localization of a gene for autosomal dominant Larsen syndrome to chromosome region 3p21.1-14.1 in the proximity of, but distinct from, the COL7A1 locus |journal=Am. J. Hum. Genet. |volume=57 |issue= 5 |pages= 1104–13 |year= 1995 |pmid= 7485161 |doi=  | pmc=1801374  |display-authors=etal}}
*{{cite journal  | author=Leedman PJ, Faulkner-Jones B, Cram DS, ''et al.'' |title=Cloning from the thyroid of a protein related to actin binding protein that is recognized by Graves disease immunoglobulins. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=90 |issue= 13 |pages= 5994-8 |year= 1993 |pmid= 8327473 |doi= }}
*{{cite journal  |vauthors=Leedman PJ, Faulkner-Jones B, Cram DS |title=Cloning from the thyroid of a protein related to actin binding protein that is recognized by Graves disease immunoglobulins |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=90 |issue= 13 |pages= 5994–8 |year= 1993 |pmid= 8327473 |doi=10.1073/pnas.90.13.5994  | pmc=46853  |display-authors=etal}}
*{{cite journal  | author=Zhang W, Han SW, McKeel DW, ''et al.'' |title=Interaction of presenilins with the filamin family of actin-binding proteins. |journal=J. Neurosci. |volume=18 |issue= 3 |pages= 914-22 |year= 1998 |pmid= 9437013 |doi=  }}
*{{cite journal  |vauthors=Zhang W, Han SW, McKeel DW |title=Interaction of presenilins with the filamin family of actin-binding proteins |journal=J. Neurosci. |volume=18 |issue= 3 |pages= 914–22 |year= 1998 |pmid= 9437013 |doi=  | pmc=2042137  |display-authors=etal}}
*{{cite journal  | author=Takafuta T, Wu G, Murphy GF, Shapiro SS |title=Human beta-filamin is a new protein that interacts with the cytoplasmic tail of glycoprotein Ibalpha. |journal=J. Biol. Chem. |volume=273 |issue= 28 |pages= 17531-8 |year= 1998 |pmid= 9651345 |doi=  }}
*{{cite journal  |vauthors=Takafuta T, Wu G, Murphy GF, Shapiro SS |title=Human beta-filamin is a new protein that interacts with the cytoplasmic tail of glycoprotein Ibalpha |journal=J. Biol. Chem. |volume=273 |issue= 28 |pages= 17531–8 |year= 1998 |pmid= 9651345 |doi=10.1074/jbc.273.28.17531 }}
*{{cite journal  | author=Xu W, Xie Z, Chung DW, Davie EW |title=A novel human actin-binding protein homologue that binds to platelet glycoprotein Ibalpha. |journal=Blood |volume=92 |issue= 4 |pages= 1268-76 |year= 1998 |pmid= 9694715 |doi=  }}
*{{cite journal  |vauthors=Xu W, Xie Z, Chung DW, Davie EW |title=A novel human actin-binding protein homologue that binds to platelet glycoprotein Ibalpha |journal=Blood |volume=92 |issue= 4 |pages= 1268–76 |year= 1998 |pmid= 9694715 |doi=  }}
*{{cite journal  | author=Bröcker F, Bardenheuer W, Vieten L, ''et al.'' |title=Assignment of human filamin gene FLNB to human chromosome band 3p14.3 and identification of YACs containing the complete FLNB transcribed region. |journal=Cytogenet. Cell Genet. |volume=85 |issue= 3-4 |pages= 267-8 |year= 1999 |pmid= 10449914 |doi=  }}
*{{cite journal  |vauthors=Bröcker F, Bardenheuer W, Vieten L |title=Assignment of human filamin gene FLNB to human chromosome band 3p14.3 and identification of YACs containing the complete FLNB transcribed region |journal=Cytogenet. Cell Genet. |volume=85 |issue= 3–4 |pages= 267–8 |year= 1999 |pmid= 10449914 |doi=10.1159/000015309 |display-authors=etal}}
*{{cite journal  | author=Ikeda K, Takahashi Y, Katagiri S |title=Effect of medium change on the development of in vitro matured and fertilized bovine oocytes cultured in medium containing amino acids. |journal=J. Vet. Med. Sci. |volume=62 |issue= 1 |pages= 121-3 |year= 2000 |pmid= 10676904 |doi= }}
*{{cite journal  |vauthors=Ikeda K, Takahashi Y, Katagiri S |title=Effect of medium change on the development of in vitro matured and fertilized bovine oocytes cultured in medium containing amino acids |journal=J. Vet. Med. Sci. |volume=62 |issue= 1 |pages= 121–3 |year= 2000 |pmid= 10676904 |doi=10.1292/jvms.62.121  }}
*{{cite journal  | author=Chakarova C, Wehnert MS, Uhl K, ''et al.'' |title=Genomic structure and fine mapping of the two human filamin gene paralogues FLNB and FLNC and comparative analysis of the filamin gene family. |journal=Hum. Genet. |volume=107 |issue= 6 |pages= 597-611 |year= 2001 |pmid= 11153914 |doi=  }}
*{{cite journal  |vauthors=Chakarova C, Wehnert MS, Uhl K |title=Genomic structure and fine mapping of the two human filamin gene paralogues FLNB and FLNC and comparative analysis of the filamin gene family |journal=Hum. Genet. |volume=107 |issue= 6 |pages= 597–611 |year= 2001 |pmid= 11153914 |doi=10.1007/s004390000414 |display-authors=etal}}
*{{cite journal  | author=Dyson JM, O'Malley CJ, Becanovic J, ''et al.'' |title=The SH2-containing inositol polyphosphate 5-phosphatase, SHIP-2, binds filamin and regulates submembraneous actin. |journal=J. Cell Biol. |volume=155 |issue= 6 |pages= 1065-79 |year= 2002 |pmid= 11739414 |doi= 10.1083/jcb.200104005 }}
*{{cite journal  |vauthors=Dyson JM, O'Malley CJ, Becanovic J |title=The SH2-containing inositol polyphosphate 5-phosphatase, SHIP-2, binds filamin and regulates submembraneous actin |journal=J. Cell Biol. |volume=155 |issue= 6 |pages= 1065–79 |year= 2002 |pmid= 11739414 |doi= 10.1083/jcb.200104005 | pmc=2150887 |display-authors=etal}}
*{{cite journal  | author=van der Flier A, Kuikman I, Kramer D, ''et al.'' |title=Different splice variants of filamin-B affect myogenesis, subcellular distribution, and determine binding to integrin [beta] subunits. |journal=J. Cell Biol. |volume=156 |issue= 2 |pages= 361-76 |year= 2002 |pmid= 11807098 |doi= 10.1083/jcb.200103037 }}
*{{cite journal  |vauthors=van der Flier A, Kuikman I, Kramer D |title=Different splice variants of filamin-B affect myogenesis, subcellular distribution, and determine binding to integrin [beta] subunits |journal=J. Cell Biol. |volume=156 |issue= 2 |pages= 361–76 |year= 2002 |pmid= 11807098 |doi= 10.1083/jcb.200103037 | pmc=2199218 |display-authors=etal}}
*{{cite journal  | author=Donaldson JC, Dise RS, Ritchie MD, Hanks SK |title=Nephrocystin-conserved domains involved in targeting to epithelial cell-cell junctions, interaction with filamins, and establishing cell polarity. |journal=J. Biol. Chem. |volume=277 |issue= 32 |pages= 29028-35 |year= 2002 |pmid= 12006559 |doi= 10.1074/jbc.M111697200 }}
*{{cite journal  |vauthors=Donaldson JC, Dise RS, Ritchie MD, Hanks SK |title=Nephrocystin-conserved domains involved in targeting to epithelial cell-cell junctions, interaction with filamins, and establishing cell polarity |journal=J. Biol. Chem. |volume=277 |issue= 32 |pages= 29028–35 |year= 2002 |pmid= 12006559 |doi= 10.1074/jbc.M111697200 }}
*{{cite journal  | author=Shoeman RL, Hartig R, Hauses C, Traub P |title=Organization of focal adhesion plaques is disrupted by action of the HIV-1 protease. |journal=Cell Biol. Int. |volume=26 |issue= 6 |pages= 529-39 |year= 2003 |pmid= 12119179 |doi=  }}
*{{cite journal  |vauthors=Shoeman RL, Hartig R, Hauses C, Traub P |title=Organization of focal adhesion plaques is disrupted by action of the HIV-1 protease |journal=Cell Biol. Int. |volume=26 |issue= 6 |pages= 529–39 |year= 2003 |pmid= 12119179 |doi=10.1006/cbir.2002.0895 }}
*{{cite journal  | author=Sheen VL, Feng Y, Graham D, ''et al.'' |title=Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interact. |journal=Hum. Mol. Genet. |volume=11 |issue= 23 |pages= 2845-54 |year= 2003 |pmid= 12393796 |doi= }}
*{{cite journal  |vauthors=Sheen VL, Feng Y, Graham D |title=Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interact |journal=Hum. Mol. Genet. |volume=11 |issue= 23 |pages= 2845–54 |year= 2003 |pmid= 12393796 |doi=10.1093/hmg/11.23.2845  |display-authors=etal}}
*{{cite journal  | author=Takafuta T, Saeki M, Fujimoto TT, ''et al.'' |title=A new member of the LIM protein family binds to filamin B and localizes at stress fibers. |journal=J. Biol. Chem. |volume=278 |issue= 14 |pages= 12175-81 |year= 2003 |pmid= 12496242 |doi= 10.1074/jbc.M209339200 }}
*{{cite journal  |vauthors=Takafuta T, Saeki M, Fujimoto TT |title=A new member of the LIM protein family binds to filamin B and localizes at stress fibers |journal=J. Biol. Chem. |volume=278 |issue= 14 |pages= 12175–81 |year= 2003 |pmid= 12496242 |doi= 10.1074/jbc.M209339200 |display-authors=etal}}
*{{cite journal  | author=Himmel M, Van Der Ven PF, Stöcklein W, Fürst DO |title=The limits of promiscuity: isoform-specific dimerization of filamins. |journal=Biochemistry |volume=42 |issue= 2 |pages= 430-9 |year= 2003 |pmid= 12525170 |doi= 10.1021/bi026501+ }}
*{{cite journal  |vauthors=Himmel M, Van Der Ven PF, Stöcklein W, Fürst DO |title=The limits of promiscuity: isoform-specific dimerization of filamins |journal=Biochemistry |volume=42 |issue= 2 |pages= 430–9 |year= 2003 |pmid= 12525170 |doi= 10.1021/bi026501+}}
*{{cite journal  | author=Ota T, Suzuki Y, Nishikawa T, ''et al.'' |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40-5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 }}
*{{cite journal  |vauthors=Ota T, Suzuki Y, Nishikawa T |title=Complete sequencing and characterization of 21,243 full-length human cDNAs |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 |display-authors=etal}}
}}
}}
{{refend}}
{{refend}}
 
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Revision as of 15:58, 25 November 2017

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

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RefSeq (protein)

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Filamin B, beta (FLNB), also known as Filamin B, beta (actin binding protein 278), is a cytoplasmic protein which in humans is encoded by the FLNB gene.

FLNB regulates intracellular communication and signalling by cross-linking the protein actin to allow direct communication between the cell membrane and cytoskeletal network, to control and guide proper skeletal development.[1]

Mutations in the FLNB gene are involved in several lethal bone dysplasias, including boomerang dysplasia and atelosteogenesis type I.[2][3][4]


Interactions

FLNB has been shown to interact with GP1BA,[5] Filamin,[6] FBLIM1,[7] PSEN1,[8] CD29[9] and PSEN2.[8]

See also

References

  1. Lu J, Lian G, Lenkinski R, De Grand A, Vaid RR, Bryce T, Stasenko M, Boskey A, Walsh C, Sheen V (2007). "Filamin B mutations cause chondrocyte defects in skeletal development". Hum Mol Genet. 16 (14): 1661–1675. doi:10.1093/hmg/ddm114. PMID 17510210.
  2. Bicknell LS, Morgan T, Bonife L, Wessels MW, Bialer MG, Willems PJ, Cohen DH, Krakow D, Robertson SP (2005). "Mutations in FLNB cause boomerang dysplasia". Am J Med Genet. 42 (7): e43. doi:10.1136/jmg.2004.029967. PMC 1736093. PMID 15994868.
  3. Greally MT; Jewett T; Smith WL Jr.; Penick GD; Williamson RA (1993). "Lethal bone dysplasia in a fetus with manifestations of Atelosteogenesis type I and Boomerang dysplasia". Am J Med Genet. 47 (4): 1086–1091. doi:10.1002/ajmg.1320470731. PMID 8291529.
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